MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Disease: Neural Tube Defects ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4242182
rs4242182
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
CUI: C0027794
Disease:
Neural Tube Defects 		0.010 GeneticVariation BEFREE Maternal Msx2 C386T gene polymorphisms were associated with fetal neural tube defects in Han Chinese women in Shanxi Province. 21362336 2011